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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pseudohypoaldosteronism type 2E
Multiple myeloma

CUL3 CCND1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CUL3
(0.52)
CCND1



Citations in the biomedical literature:


Pseudohypoaldosteronism type 2E
CUL3
Multiple myeloma
CCND1



Pseudohypoaldosteronism type 2E
Multiple myeloma

Synonym(s):
- PHA2E

Synonym(s):
- Kahler's disease
- Medullary plasmacytoma
- Myelomatosis
- Plasma cell myeloma

Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D009101

No signs/symptoms info available.